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J.1365-2141.2002.03368.X
J.1365-2141.2002.03368.X
http://dx.doi.org/10.1046/J.1365-2141.2002.03368.X
Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.
P356
Q43936473-D53FD96F-393C-461F-88D7-8637FA638628
P356
J.1365-2141.2002.03368.X
http://dx.doi.org/10.1046/J.1365-2141.2002.03368.X